Mapping Data

Experiment

• Experiment
  TEXT
• Chromosome
  7
• Reference
  J:61682 Hagiwara N, et al., Sox6 is a candidate gene for p100H myopathy, heart block, and sudden neonatal death. Proc Natl Acad Sci U S A. 2000 Apr 11;97(8):4180-5
• ID
  MGI:1855706

Genes

Gene	Assay Type
Oca2	PCR amplified length variant
Sox6	PCR amplified length variant

Notes

• Experiment
  Authors provided evidence using karyotyping and RT-PCR showing that the p^100H mutation is the result of an inversion within the Sox6 gene on mouse Chromosome 7. The breakpoint of the inversion is within band 7B5 and 7F1.